| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:55534646-55534678 | Common:1; Rare:15 | ||||
| chr5:55534683-55534799 | Common:1; Rare:40 | ||||
| chr5:55994782-55995182 | Common:1; Rare:131 | ||||
| chr5:56909396-56909648 | Common:4; Rare:69 | ||||
| chr5:56952109-56952298 | Rare:68 | ||||
| chr5:57173551-57173858 | Common:2; Rare:108 | ||||
| chr5:58459807-58460246 | Common:7; Rare:168 | ||||
| chr5:60945031-60945258 | Common:4; Rare:85; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:61162395-61162499 | Common:1; Rare:27 | ||||
| chr5:62306367-62306485 | Rare:33; Clinvar (benign):2 | ||||
| chr5:62403508-62403525 | Rare:2 | ||||
| chr5:62403800-62404032 | Common:3; Rare:87 | ||||
| chr5:62412596-62412799 | Common:1; Rare:61 | ||||
| chr5:64768513-64768977 | Common:5; Rare:128 | ||||
| chr5:65563101-65563316 | Common:4; Rare:78 |